ClinVar Miner

Submissions for variant NM_021008.4(DEAF1):c.970T>A (p.Leu324Met)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV003148272 SCV003834978 uncertain significance Intellectual disability, autosomal dominant 24 2021-01-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003778889 SCV004680842 likely benign not provided 2024-05-15 criteria provided, single submitter clinical testing

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